Future rheumatology最新文献

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Is aspirin treatment an appropriate intervention to osteoporosis? 阿司匹林治疗是骨质疏松症的适当干预吗?
Future rheumatology Pub Date : 2008-12-01 DOI: 10.2217/17460816.3.6.499
Songtao Shi, Takayoshi Yamaza, Kentaro Akiyama
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引用次数: 17
Heart rate variability as a biomarker of fibromyalgia syndrome. 心率变异性作为纤维肌痛综合征的生物标志物。
Future rheumatology Pub Date : 2008-10-01 DOI: 10.2217/17460816.3.5.475
Roland Staud
{"title":"Heart rate variability as a biomarker of fibromyalgia syndrome.","authors":"Roland Staud","doi":"10.2217/17460816.3.5.475","DOIUrl":"https://doi.org/10.2217/17460816.3.5.475","url":null,"abstract":"<p><p>Fibromyalgia (FM) is a chronic pain syndrome characterized by widespread mechanical tenderness, fatigue, nonrefreshing sleep and depressed mood. Several biological abnormalities have been described in FM patients, including elevated substance P in the cerebrospinal fluid, increased CNS sensitivity to painful and nonpainful stimuli and pervasive dysfunction of the autonomic nervous system (ANS). Such ANS abnormalities include, but are not limited to: tachycardia, postural intolerance, Raynaud's phenomenon, and diarrhea or constipation. Heart rate variability (HRV) analysis of FM patients can be used to assess ANS dysfunction, specifically related to sympathovagal balance, which has provided evidence for nonabating sympathetic hyperactivity in this chronic pain population. Although not specific for FM, ANS dysfunction can be readily determined by HRV analysis requiring only computer analysis of electrocardiogram recordings by commercially available software. HRV has been shown to correlate with FM pain and is sensitive to change; in particular, pain related to physical and mental stressors. Thus, ANS dysfunction as assessed by HRV analysis may serve as a useful biomarker, and may become part of future FM diagnostic criteria and serve as a surrogate end point in clinical trials.</p>","PeriodicalId":88490,"journal":{"name":"Future rheumatology","volume":"3 5","pages":"475-483"},"PeriodicalIF":0.0,"publicationDate":"2008-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.2217/17460816.3.5.475","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"28489086","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 81
Imaging in ankylosing spondylitis 强直性脊柱炎的影像学表现
Future rheumatology Pub Date : 2007-04-01 DOI: 10.2217/17460816.2.2.115
W. Maksymowych
{"title":"Imaging in ankylosing spondylitis","authors":"W. Maksymowych","doi":"10.2217/17460816.2.2.115","DOIUrl":"https://doi.org/10.2217/17460816.2.2.115","url":null,"abstract":"Clinicians and researchers have turned to imaging to address several major challenges in the clinical evaluation and treatment of ankylosing spondylitis (AS). The advent of more effective therapies targeting the pro-inflammatory cytokine tumor necrosis factor (TNF)-α has provided a more justifiable need to establish a diagnosis early in the disease course, particularly if it can be shown that such therapies have disease-modifying potential. Unfortunately, symptom duration prior to diagnosis of AS remains stubbornly at 8–9 years in most advanced countries [1]. This reflects the low discriminant value of the history in distinguishing between inflammatory and mechanical causes of back pain [2], the lack of physical signs related to spinal and sacroiliac joint inflammation in early disease, and the low sensitivity and specificity of laboratory abnormalities that are confined to acute-phase reactants [3]. The same limitations preclude objective evaluation of disease activity in patients with established disease. The advent of magnetic resonance imaging (MRI) has proven to be a milestone in the field, through its ability to permit direct visualization of inflammatory lesions in the spine and sacroiliac joints. Scoring systems that permit quantification of the degree of inflammation on MRI scans have also been developed, which now allow the objective analysis of disease severity in longitudinal studies and in clinical trials evaluating the efficacy of new antiinflammatory agents. Advances in the use of other imaging modalities have been more limited and primarily confined to the development of a scoring tool to quantify structural damage on plain radiography of the spine. This tool is now being used to assess the disease-modifying potential of standard therapies, such as nonsteroidal antiinflammatory agents, as well as anti-TNF-α therapies. Although it is now undeniable that advances in imaging have enhanced their value to both the clinician and the researcher, there has been insufficient awareness of the pitfalls inherent to the use of these imaging modalities in the setting of AS. The primary advantage of MRI is its ability to visualize lesions within soft tissues and bone in 3D. T1-weighted sequences primarily detect the signal from fat, and the contrast with bone, which is dark, enhances anatomical delineation of joint structures. T2-weighted sequences suppress the signal from fat that is present in bone marrow, allowing visualization of an underlying water signal that may be related to inflammation, cyst, tumor and other pathologies associated with increased vascular permeability. The two images should be analyzed simultaneously as they provide complementary information. For example, loss of the fat signal in subchondral bone marrow on the T1 image of the sacroiliac joint, accompanied by a corresponding water signal on the T2 image, typically denotes inflammation.","PeriodicalId":88490,"journal":{"name":"Future rheumatology","volume":"21 1","pages":"115-119"},"PeriodicalIF":0.0,"publicationDate":"2007-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"89075312","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 20
Pediatric systemic lupus erythematosus 小儿系统性红斑狼疮
Future rheumatology Pub Date : 2007-02-05 DOI: 10.1007/978-1-84800-934-9_14
E. Silverman
{"title":"Pediatric systemic lupus erythematosus","authors":"E. Silverman","doi":"10.1007/978-1-84800-934-9_14","DOIUrl":"https://doi.org/10.1007/978-1-84800-934-9_14","url":null,"abstract":"","PeriodicalId":88490,"journal":{"name":"Future rheumatology","volume":"2 1","pages":"161-167"},"PeriodicalIF":0.0,"publicationDate":"2007-02-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1007/978-1-84800-934-9_14","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"51065339","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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